3',6'-Dimethoxy-3h-spiro[isobenzofuran-1,9'-xanthen]-3-one CAS 36886-76-7

Purity 97%+In StockPharmaceutical Standards
CAS No.36886-76-7
Molecular FormulaC22H16O5
Molecular Weight360.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3',6'-Dimethoxy-3h-spiro[isobenzofuran-1,9'-xanthen]-3-one CAS 36886-76-7 chemical structure

Description

3',6'-Dimethoxy-3h-spiro[isobenzofuran-1,9'-xanthen]-3-one (C22H16O5) contains a flavonoid core, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies 3',6'-Dimethoxy-3h-spiro[isobenzofuran-1,9'-xanthen]-3-one (CAS 36886-76-7), a certified reference material (molecular formula C22H16O5, MW 360.36 g/mol) for analytical method development and quality control.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures 3',6'-Dimethoxy-3h-spiro[isobenzofuran-1,9'-xanthen]-3-one under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC22H16O5
Molecular Weight360.36 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1967

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